121 research outputs found

    Diffractive parton distributions from the saturation model

    Get PDF
    We review diffractive deep inelastic scattering (DIS) in the light of the collinear factorization theorem. This theorem allows to define diffractive parton distributions in the leading twist approach. Due to its selective final states, diffractive DIS offers interesting insight into the form of the diffractive parton distributions which we explore with the help of the saturation model. We find Regge-like factorization with the correct energy dependence measured at HERA. A remarkable feature of diffractive DIS is the dominance of the twist-4 contribution for small diffractive masses. We quantify this effect and make a comparison with the data.Comment: 18 pages, 6 figures, latex, Q_0^2 corrected in comparison to the journal versio

    Femtosecond manipulation of spins, charges, and ions in nanostructures, thin films, and surfaces

    Full text link
    Modern ultrafast techniques provide new insights into the dynamics of ions, charges, and spins in photoexcited nanostructures. In this review, we describe the use of time-resolved electron-based methods to address specific questions such as the ordering properties of self-assembled nanoparticles supracrystals, the interplay between electronic and structural dynamics in surfaces and adsorbate layers, the light-induced control of collective electronic modes in nanowires and thin films, and the real-space/real-time evolution of the skyrmion lattice in topological magnets

    Energy-dependent photoemission delays from noble metal surfaces by attosecond interferometry

    Full text link
    How quanta of energy and charge are transported on both atomic spatial and ultrafast time scales is at the heart of modern technology. Recent progress in ultrafast spectroscopy has allowed us to directly study the dynamical response of an electronic system to interaction with an electromagnetic field. Here, we present energy-dependent photoemission delays from the noble metal surfaces Ag(111) and Au(111). An interferometric technique based on attosecond pulse trains is applied simultaneously in a gas phase and a solid state target to derive surface-specific photoemission delays. Experimental delays on the order of 100 as are in the same time range as those obtained from simulations. The strong variation of measured delays with excitation energy in Ag(111), which cannot be consistently explained invoking solely electron transport or initial state localization as supposed in previous work, indicates that final state effects play a key role in photoemission from solids

    Renormalization of spectral lineshape and dispersion below Tc in Bi2Sr2CaCu2O8+d

    Full text link
    Angle-resolved photoemission (ARPES) data in the superconducting state of Bi2Sr2CaCu2O8+d show a kink in the dispersion along the zone diagonal, which is related via a Kramers-Kronig analysis to a drop in the low-energy scattering rate. As one moves towards (pi,0), this kink evolves into a spectral dip. The occurrence of these anomalies in the dispersion and lineshape throughout the zone indicate the presence of a new energy scale in the superconducting state.Comment: New Figure 3 with expanded discussio

    Robustness of the charge-ordered phases in IrTe2_2 against photoexcitation

    Full text link
    We present a time-resolved angle-resolved photoelectron spectroscopy study of IrTe2_2, which undergoes two first-order structural and charge-ordered phase transitions on cooling below 270 K and below 180 K. The possibility of inducing a phase transition by photoexcitation with near-infrared femtosecond pulses is investigated in the charge-ordered phases. We observe changes of the spectral function occuring within a few hundreds of femtoseconds and persisting up to several picoseconds, which we interpret as a partial photoinduced phase transition (PIPT). The necessary time for photoinducing these spectral changes increases with increasing photoexcitation density and reaches timescales longer than the rise time of the transient electronic temperature. We conclude that the PIPT is driven by a transient increase of the lattice temperature following the energy transfer from the electrons. However, the photoinduced changes of the spectral function are small, which indicates that the low temperature phase is particularly robust against photoexcitation. We suggest that the system might be trapped in an out-of-equilibrium state, for which only a partial structural transition is achieved.Comment: 8 pages, 5 figures, accepted for publication in Phys. Rev.

    Robustness of the charge-ordered phases in IrTe2{\mathrm{IrTe}}_{2} against photoexcitation

    Get PDF
    We present a time-resolved angle-resolved photoelectron spectroscopy study of IrTe2, which undergoes two first-order structural and charge-ordered phase transitions on cooling below 270 K and below 180 K. The possibility of inducing a phase transition by photoexcitation with near-infrared femtosecond pulses is investigated in the charge-ordered phases. We observe changes of the spectral function occurring within a few hundreds of femtoseconds and persisting up to several picoseconds, which we interpret as a partial photoinduced phase transition (PIPT). The necessary time for photoinducing these spectral changes increases with increasing photoexcitation density and reaches time scales longer than the rise time of the transient electronic temperature. We conclude that the PIPT is driven by a transient increase of the lattice temperature following the energy transfer from the electrons. However, the photoinduced changes of the spectral function are small, which indicates that the low- temperature phase is particularly robust against photoexcitation. We suggest that the system might be trapped in an out-of-equilibrium state, for which only a partial structural transition is achieved

    Electron-phonon renormalization in small Fermi energy systems

    Full text link
    The puzzling features of recent photoemission data in cuprates have been object of several analysis in order to identity the nature of the underlying electron-boson interaction. In this paper we point out that many basilar assumptions of the conventional analysis as expected to fail in small Fermi energy systems when, as the cuprates, the Fermi energy EFE_{\rm F} is comparable with the boson energy scale. We discuss in details the novel features appearing in the self-energy of small Fermi energy systems and the possible implications on the ARPES data in cuprates.Comment: 4 pages, 5 eps figures include

    Delayed electron emission in strong-field driven tun-nelling from a metallic nanotip in the multi-electronregime

    Get PDF
    Illuminating a nano-sized metallic tip with ultrashort laser pulses leads to the emission of electrons due to multiphoton excitations. As optical fields become stronger, tunnelling emission directly from the Fermi level becomes prevalent. This can generate coherent electron waves in vacuum leading to a variety of attosecond phenomena. Working at high emission currents where multi-electron effects are significant, we were able to characterize the transition from one regime to the other. Specifically, we found that the onset of laser-driven tunnelling emission is heralded by the appearance of a peculiar delayed emission channel. In this channel, the electrons emitted via laser-driven tunnelling emission are driven back into the metal, and some of the electrons reappear in the vacuum with some delay time after undergoing inelastic scattering and cascading processes inside the metal. Our understanding of these processes gives insights on attosecond tunnelling emission from solids and should prove useful in designing new types of pulsed electron sources.111410Ysciescopu

    Ferrule-top nanoindenter: An optomechanical fiber sensor for nanoindentation

    Get PDF
    Ferrule-top probes are self-aligned all-optical devices obtained by fabricating a cantilever on the top of a ferruled optical fiber. This approach has been proven to provide a new platform for the realization of small footprint atomic force microscopes (AFMs) that adapt well to utilization outside specialized laboratories [D. Chavan, Rev. Sci. Instrum. 81, 123702 (2010)10.1063/1.3516044; D. Chavan, Rev. Sci. Instrum. 82, 046107 (2011)10.1063/1.3579496]. In this paper we now show that ferrule-top cantilevers can be also used to develop nanoindenters. Our instrument combines the sensitivity of commercial AFM-based indentation with the ease-of-use of more macroscopic instrumented indenters available today on the market. Furthermore, the all-optical design allows smooth operations also in liquids, where other devices are much more limited and often provide data that are difficult to interpret. This study may pave the way to the implementation of a new generation user-friendly nanoindenters for the measurement of the stiffness of samples in material sciences and medical research. © 2012 American Institute of Physics
    • 

    corecore